Details

Autor(en) / Beteiligte

• Lindsay, Colin R
• Lawn, Samuel
• Campbell, Andrew D
• Faller, William J
• Rambow, Florian
• Mort, Richard L
• Timpson, Paul
• Li, Ang
• Cammareri, Patrizia
• Ridgway, Rachel A
• Morton, Jennifer P
• Doyle, Brendan
• Hegarty, Shauna
• Rafferty, Mairin
• Murphy, Ian G
• McDermott, Enda W
• Sheahan, Kieran
• Pedone, Katherine
• Finn, Alexander J
• Groben, Pamela A
• Thomas, Nancy E
• Hao, Honglin
• Carson, Craig
• Norman, Jim C
• Machesky, Laura M
• Gallagher, William M
• Jackson, Ian J
• Van Kempen, Leon
• Beermann, Friedrich
• Der, Channing
• Larue, Lionel
• Welch, Heidi C
• Ozanne, Brad W
• Sansom, Owen J

Titel

P-Rex1 is required for efficient melanoblast migration and melanoma metastasis

Ist Teil von

• Nature communications, 2011-11, Vol.2 (1), p.555-555, Article 555

Ort / Verlag

England: Nature Publishing Group

Erscheinungsjahr

2011

Link zum Volltext

Quelle

Free E-Journal (出版社公開部分のみ）

Beschreibungen/Notizen

• Metastases are the major cause of death from melanoma, a skin cancer that has the fastest rising incidence of any malignancy in the Western world. Molecular pathways that drive melanoblast migration in development are believed to underpin the movement and ultimately the metastasis of melanoma. Here we show that mice lacking P-Rex1, a Rac-specific Rho GTPase guanine nucleotide exchange factor, have a melanoblast migration defect during development evidenced by a white belly. Moreover, these P-Rex1(-/-) mice are resistant to metastasis when crossed to a murine model of melanoma. Mechanistically, this is associated with P-Rex1 driving invasion in a Rac-dependent manner. P-Rex1 is elevated in the majority of human melanoma cell lines and tumour tissue. We conclude that P-Rex1 has an important role in melanoblast migration and cancer progression to metastasis in mice and humans.